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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845141Generated: October 31, 2026

4-Chlorobenzoic Acid → 4-Chloro-3-(chlorosulphonyl)benzoic acid

https://huagongshe.com/reaction/1845141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoic AcidHCID 6318—
ReactantChlorosulfonic acidHCID 24638—
Product4-Chloro-3-(chlorosulphonyl)benzoic acidHCID 75613—

Reaction Conditions

Temperature130 °C

Reaction Steps

A round bottom flask was charged with chlorosulfonic acid (6.36 g, 96.0 mmol) at 0° C. and 4-chloro benzoic acid was added portion wise. The reaction mixture was heated at 130° C. for 5 h. The reaction mixture was then poured over ice and stirred for 10 minutes. The solids formed were filtered, washed with cold water and dried to afford 4-chloro-3-(chlorosulfonyl)benzoic acid as a white powder. This compound was then charged into a round bottom flask containing sodium sulfite (7.1 g, 56.4 mmol) and water (40 mL) portion wise. Aqueous sodium hydroxide (6 N) was then added drop wise till the pH of the reaction mixture reaches 10 and the reaction was stirred over night. The reaction was then made acidic (pH 2) by addition of 2N HCl. The solids formed were filtered and dried to get the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-37453a730fef4ccf967df04ad3503386
Source noteuspto-grants-2015_02